Quality Surveillance Engineer Job at Randstad (Pune)

Senior Quality Engineer (Bulk Inspection)

We are seeking an experienced Senior Quality Engineer to support supplier manufa...

Location

United Kingdom , Bradford

Salary:

Not provided

ASSYSTEM

Expiration Date

Until further notice

Requirements

Qualification in an Engineering discipline (ONC / HNC / HND / Degree or equivalent experience)
Experience in a quality inspection or supplier quality role within engineering or manufacturing
Significant experience in quality inspection or quality engineering within a manufacturing environment
Experience overseeing supplier manufacturing and inspection activities
Strong understanding of engineering drawings, specifications and inspection requirements
Experience working to UK and international engineering standards and codes
Ability to identify, document and manage non-conformances and corrective actions
Experience supporting quality surveillance programmes and supplier oversight

Job Responsibility

Perform supplier inspections and witnessing activities in line with Inspection & Test Plans (ITPs)
Verify that manufactured equipment and components meet contract specifications, drawings and applicable standards
Review supplier quality documentation and manufacturing records prior to product release
Identify, raise and track non-conformances, ensuring appropriate corrective actions are implemented
Accept or reject manufactured items based on inspection outcomes
Work closely with suppliers to ensure quality requirements are fully understood and implemented
Support the development and delivery of the supplier surveillance and inspection programme
Produce inspection reports and summary updates highlighting quality performance and key issues
Ensure compliance with relevant national and international engineering standards
Collaborate with project quality leads to ensure effective quality oversight across the supply chain

What we offer

Hybrid Working – Flexibility to work from home and the office
25 Days Annual Leave + Bank Holidays
Buy & Sell Holiday – Make your time off work for you
8% Company Pension Contributions
Income Protection & 3x Salary Death-in-Service Cover
Competitive Sick Pay – Support when you need it
Healthcare Cash Plan – Claim back on dental, optical & more
Free Digital Gym Access – Expert-led fitness classes
Exclusive Discounts – Restaurants, days out & top brands
24/7 Employee Support Line – Mental health, financial & legal help

Fulltime

Quality Manager

Location

Brunei

Salary:

Not provided

Bureau Veritas Certification CZ, s.r.o.

Expiration Date

Until further notice

Requirements

Degree or Diploma in Mechanical, Materials, Quality, or related engineering discipline
ISO 9001 Lead Auditor certification (mandatory)
Minimum 7–10 years experience in QA/QC, inspection, or quality management within the Oil & Gas or critical asset industries
Strong understanding of: ISO 9001 Quality Management Systems, ISO 17020 (Inspection Bodies), ISO 17025 calibration requirements, API/ASME inspection codes and COMPANY quality standards
Familiar with NDT/Advanced NDT competency standards (ISO 9712, SNT-TC-1A, CSWIP, API 570/510/653)
Experience with Vendor Inspection, fabrication surveillance, and document review
Strong analytical, audit, and problem-solving capabilities (NCR, RCA, CAR processes)
Proficient in MS Office, digital inspection systems, and quality management tools
Effective communication and stakeholder management skills to interface with COMPANY representatives
HSSE awareness and required COMPANY training (BOSIET if offshore visits are required)

Job Responsibility

Provide overall leadership and governance of the Contractor Quality Management System (QMS) to ensure full compliance with COMPANY requirements, ISO 9001, and ISO 17020
Oversee all quality functions including: Quality Assurance Engineer, Tools, Materials & Calibration Coordinator, Vendor Third-Party Inspection (VTPI) Coordinator, Quality Engineering Team (Quality Lead, Senior QAQC Engineer, Project QE, QCS Engineer)
Ensure all inspection deliverables, reports, data submissions, workpacks, and documentation meet COMPANY quality standards, procedures, and contractual obligations
Lead the preparation, submission, implementation, and maintenance of the Quality Assurance Plan (QAP), ITPs, Surveillance Plan, and contract-specific quality documentation
Manage and execute internal quality audits, support COMPANY audits, and ensure timely closure of NCRs, CARs, and preventive actions
Ensure calibration compliance of all NDT/Advanced NDT equipment, gauges, EX-rated devices, and inspection tools in accordance with ISO 17025 requirements
Provide quality oversight for Vendor Inspection / TPI activities, including review of Vendor Quality Plans, ITPs, FAT/SAT procedures, and manufacturing surveillance reports
Review and validate inspection data quality, ensuring accuracy, completeness, traceability, and compliance before CIRRAS/SAP submission
Lead quality risk assessments, identify quality gaps, and implement improvements to enhance reliability of inspection execution
Ensure personnel competency and qualification records for inspection/NDT staff are maintained in accordance with contract requirements (ISO 9712, API, CSWIP, ASNT, IRATA)

Principal Quality Engineer (Quality Management Lead)

We are recruiting Principal Quality Engineers (PQEs) to support the Sizewell C (...

Location

United Kingdom , London; Bristol; Suffolk (Sizewell C site); Manchester

Salary:

Not provided

ASSYSTEM

Expiration Date

Until further notice

Requirements

Background in large, complex and highly regulated environments—ideally in nuclear or similarly regulated sectors—with strong focus on project quality and expertise in a relevant engineering discipline (mechanical, electrical, I&C, fabrication)
Strong understanding of Quality Assurance and Quality Control across engineering, procurement, manufacturing, construction and commissioning
Knowledge of the nuclear sector (preferably new build) and familiarity with Licence Conditions LC6, LC17 and ONR TAG 077 is desirable
Clear understanding of quality management best practice for deployment in large, complex, contract-led organisations
Confident communicator with strong presentation skills, comfortable engaging with individuals, small groups and large audiences
Experience ensuring compliance with national and international standards such as GS‑R‑3, ISO 9001, ISO 19443, ISO 3834 and EN10204
Proven ability to plan and conduct internal and supplier audits
Able to carry out unsupervised inspections to appropriate standards (e.g., pressurised systems)
Experienced in reviewing quality records (e.g., material certification, CFSI) and analysing quality data across an organisation
Experience managing people or leading teams

Job Responsibility

Support development and implementation of QA/QC arrangements across SZC
Identify and conduct supplier audits, and close out findings
Manage quality execution and support supplier technical assessments
Oversee manufacturing and construction surveillance
Manage non-conformances and Quality Release Certificate processes
Drive improvements in quality implementation across the project
Review, accept and monitor Contractors’ Quality Assurance Plans (CQAPs)
Produce and implement Project Quality Control Plans
Ensure deployment of key contractual quality arrangements (GQAS, LTQRs, ITP specifications)
Guide contractors on quality requirements and project-specific arrangements

What we offer

Hybrid Working Opportunity
Flexible working hours – 2/3 days per week in the Bristol office
Market Leading Pension scheme (8% company contribution / 4% personal contribution)
25 days’ paid annual leave + bank holidays + option to buy or sell days
Professional fees reimbursed
Employee referral scheme
Competitive Sick Pay – Support when you need it
Income Protection & 3x Salary Death-in-Service Cover
Free Digital Gym Access – Expert-led fitness classes
24/7 Employee Support Line – Mental health, financial & legal help

Fulltime

Senior Quality Engineer

Being an Engineer at Baxter means you play a critical role in helping us achieve...

Location

United States , Saint Paul

Salary:

88000.00 - 121000.00 USD / Year

Baxter

Expiration Date

Until further notice

Requirements

BS in Engineering or related field of science
3 - 5 years of experience in Manufacturing Quality, Design Assurance or Quality Systems
Excellent oral and written communication skills
Strong problem solving, technical writing and organizational skills
Self-motivated worker, persistent, curious
Working knowledge of FDA GMP and ISO 13485 requirements
Knowledge of statistics and quality tools such as SPC, Risk Analysis, Process Capability, DOE, TQM methods, and Lean/Six-Sigma
Working knowledge of MS Word, Excel, and Project applications
Display a solid technical understanding of engineering principles and procedures

Job Responsibility

Provide Quality Engineering support to manufacturing and new product development teams through Engineering Investigations, Qualifications and Validations
Identify quality issues, participate in quality improvement projects and quality activities that impact manufacturing
Responsible for preparation of written Engineering Investigation, Qualification and Validation plans, statistical analysis of data and preparation of reports to support manufacturing improvements, on-going validations, and new product development efforts
Provide quality engineering support for manufacturing lines, including floor support
Investigate and disposition nonconforming material reports (NCR events)
Initiate, investigate, and implement corrective and preventive actions as assigned
Provide quality engineering support for material nonconformances including supplier corrective actions
Support product development teams to develop new products and transfer to manufacturing through participation/leadership of risk management activities, performance of component qualifications, and execution of test protocols
Responsible for coordination of validation activities performed to ensure adherence to specifications and expectations
Initiate documentation changes and/or change control for products and processes as required to reflect validation/qualification activities and results

What we offer

Support for Parents
Continuing Education/ Professional Development
Employee Heath & Well-Being Benefits
Paid Time Off
2 Days a Year to Volunteer
medical and dental coverage that start on day one
insurance coverage for basic life, accident, short-term and long-term disability, and business travel accident insurance
Employee Stock Purchase Plan (ESPP)
401(k) Retirement Savings Plan (RSP)
Flexible Spending Accounts

Fulltime

Quality Engineer for AIT

The jobholder will be responsible for the listed activities related to quality a...

Location

Spain , Getafe Area

Salary:

Not provided

Airbus

Expiration Date

Until further notice

Requirements

Engineering degree or equivalent (Physics, Chemistry, etc.)
fluent in Spanish (at least C1)
fluent in English (at least C1)
at least 5 years of experience in the quality assurance domain for space sector projects
experience working in a cleanroom and with hardware: performing inspections, monitoring integration activities, etc.
familiarity with ECSS standards
good stakeholder management skills

Job Responsibility

Acting as the main point of contact for quality matters for the relevant project(s) throughout the assembly, integration, and test (AIT) phases, including interfacing with other departments such as Manufacturing Engineering, Materials and Processes, AIT management etc.
Performing and coordinating inspections (incoming and outgoing inspections, KIPs, MIPs)
Managing non-conformities and deviations raised during the AIT phases, including organizing, conducting, and documenting internal Non-Conformity Review Board (NRB) meetings
Preparing quality assurance documentation such as the Quality Assurance Plan, Quality Control Plan, inspection reports, etc., and contributing to other project documents such as the KIP/MIP Plan, Process Failure Mode and Effects Analysis (PFMEA), Action Plan (PA), etc.
Traveling to support test campaigns from the QA perspective (frequently abroad)
Identifying and implementing measures to reduce the cost of quality (such as reducing inspections and sampling)
Initiating and leading the Root Cause Analysis process for critical and repetitive issues in the area
Organizing and managing reviews such as Integration Readiness Reviews (IRRs)
Promoting a preventive quality mindset within the AIT team, ensuring the implementation of basic quality processes (quality authorization, quality delegation, operational surveillance, etc.)

Fulltime

Quality Manager II

Location

United States , Midland

Salary:

Not provided

Airswift Sweden

Expiration Date

Until further notice

Requirements

Experience executing project construction or quality assurance/control of engineering, procurement, and construction activities
Bachelor’s degree in Engineering or Science
Experience in responsible roles in Quality Management and coordination of quality surveillance / inspection activities for projects in the Oil and Gas Industry
Experience as a Project Quality Manager or equivalent experience in management of project quality systems for the Oil and Gas Industry
Must be proficient in common PC software (MS Word, MS Excel, etc.)
Read, write and speak fluent English
Strong leadership and communication skills
Ability to travel internationally

Job Responsibility

Provide Quality discipline input to the Project Organization Plan and manage staffing of Quality personnel for the Project Team (PT)
Develop quality plans, programs, procedures and tools to manage quality across project
Interface with other disciplines and provide Quality input to project plans
Manage the oversight of Contractors’ quality-related activities and deliverables
Act as Quality Assurance Coordinator (QAC) while none is assigned to project
Provide direction, guidance and resources to QACs
Provide advice to Project Management on quality issues and support effort to resolve them
Provide feedback on quality-related issues and metrics to the Project Quality function
Promote Quality awareness throughout the project
Prepare and maintain Project Quality Plan, Surveillance Programs and other quality procedures and tools and ensure their successful implementation across the project

Director of Quality

X-Bow Systems is hiring a Director of Quality to lead, manage, and run Quality f...

Location

United States , Luling

Salary:

200000.00 - 275000.00 USD / Year

X-Bow Systems

Expiration Date

Until further notice

Requirements

Bachelor's degree in Engineering, Quality, Manufacturing, Industrial Engineering, or a related technical field
10+ years of progressive quality leadership experience in defense, aerospace, propulsion, energetics, or another highly regulated manufacturing environment
5+ years of experience as a people manager leading quality teams at the senior manager or director level, with direct supervisory responsibility for a meaningful-sized organization rather than a small team of individual contributors
Deep knowledge of AS9100, ISO 9001, audit systems, corrective action, nonconformance control, supplier quality, and configuration-controlled manufacturing
Experience supporting U.S. government contracts and operating in highly regulated production environments
Strong understanding of inspection systems, process validation, first article inspection, traceability, and risk-based quality management
Proven ability to lead root cause investigations, drive corrective action, and improve quality performance in complex technical operations
Strong leadership, judgment, and cross-functional influence, with the ability to lead through managers and supervisors and hold teams accountable across functions and locations
U.S. Person status and ability to obtain or maintain any required security clearance or access authorization
Master's degree in Engineering, Operations, Quality, or Business Administration

Job Responsibility

Lead the company's quality organization across quality assurance, quality control, supplier quality, audit readiness, nonconformance management, and corrective action
Set quality strategy, objectives, and performance expectations aligned with operational goals, customer requirements, and company growth
Advise the COO and executive leadership on quality risks, systemic issues, compliance gaps, and improvement priorities
Own and maintain the Quality Management System across relevant operations, facilities, and programs
Ensure compliance with AS9100, ISO 9001, customer requirements, contract flow-downs, and applicable FAR/DFARS requirements
Lead internal, customer, third-party, and regulatory audit activity and maintain audit readiness
Ensure effective controls for documentation, traceability, inspection, testing, calibration, configuration control, and records retention
Lead receiving, in-process, and final inspection strategies to ensure product conformity and process discipline
Own nonconformance, containment, root cause, corrective action, and verification of effectiveness across internal and supplier issues
Improve quality performance using metrics including yield, escapes, rework, scrap, supplier defects, audit findings, and cost of poor quality

Fulltime

Systems Engineer

Joining ResMed will provide you an opportunity to make a difference in someone’s...

Location

Australia , Sydney

Salary:

Not provided

ResMed

Expiration Date

Until further notice

Requirements

Bachelor’s degree in Engineering, preferably Mechanical, Biomedical, Chemical, or Materials Engineering/Science
3–5 years of engineering experience with a systems-oriented mindset and strong analytical capabilities
Experience working within regulated industries, ideally medical devices or consumer health
Experience with requirements management, risk assessment, design control, and compliance processes in regulated environments
Familiarity with verification and validation activities, test execution, and data-driven investigations
Understanding of systems engineering principles, including requirements decomposition, interface definition, and traceability
Ability to evaluate design alternatives and assess impacts of engineering changes
Experience supporting root-cause analysis, structured problem solving, and technical investigations
Familiarity with ISO 13485, ISO 14971, regulatory audits, and quality system processes
Awareness of post-market surveillance processes and risk updates linked to field performance

Job Responsibility

Support systems engineering activities for released products, ensuring they continue to meet safety, performance, quality, and regulatory expectations across global markets
Maintain and update system requirements, design documentation, and risk files as part of sustaining engineering, ensuring changes preserve design integrity and compliance
Collaborate across engineering disciplines (Mechanical, Materials, Manufacturing, Quality, Regulatory, Supplier Quality, and Product Lifecycle Engineering) to evaluate and implement sustaining changes such as cost optimizations, supplier transitions, component updates, and compliance-driven modifications
Lead or support structured investigations into field issues, customer complaints, and post-market trends—performing root-cause analysis and contributing to effective corrective and preventive actions
Participate in post-market risk management and surveillance activities, updating risk assessments (FMEA, hazard analysis) based on field data, complaints, NCMR trends, and regulatory insights
Work closely with Verification & Validation teams to ensure system requirements are adequately tested, verified, and validated for product updates and engineering changes
Maintain full traceability and design control compliance, ensuring clear linkage between requirements, risks, specifications, and verification evidence
Support regulatory audits and inspections by preparing compliant documentation, addressing findings, and ensuring systems engineering deliverables meet ISO, FDA, and global medical device requirements
Contribute to engineering change processes, including updates to DHF/DMR, risk assessments, labeling, materials, and supplier information
Participate in cross-functional reviews, providing system-level insights for technical issues, design modifications, and sustaining decisions

What we offer

Flexible working environment
Opportunities to develop a network of like-minded people and develop further in your engineering journey

Fulltime

Quality Surveillance Engineer

Randstad

Location:
India , Pune

Category:
-

Contract Type:
Not provided

Salary:

Job Description:

Job Responsibility:

Requirements:

Additional Information:

Job Posted:
May 12, 2026

Expiration:
June 06, 2026

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